Amerikanische Gesellschaft für Hirudotherapie

Protein C.

Review published in Progress in hemostasis and thrombosis (1984)

Zuletzt aktualisiert: 18. Juni 2026Geprüft von: ASH Editorial Board
Forschungsartikel – EvidenzreviewArtikelreferenz
Evidence: Narrative reviewArzneimittelentwicklungSpeichel-PharmakologieEsmon · Progress in hemostasis and thrombosis, 1984

Abstract

The protein C anticoagulant pathway provides many new insights into control mechanisms for regulating coagulation. The observation that protein C deficiency is associated with thrombotic tendencies in the heterozygote (106-109) and early, lethal thrombosis in the homozygote (110, 111) points to the importance of the system as a major regulatory pathway. The complexity of the system has only recently begun to emerge. Thrombin activation of protein C at the endothelial cell surface requires not only the synthesis of thrombomodulin but the coupling of the receptor to a protein C binding site. It is reasonable to assume that an inherited or acquired deficiency in thrombomodulin might lead to thrombotic tendencies. This aspect of the system may explain, in part, the association between vascular disease and thrombosis. Once activated, protein C has an almost total dependence on protein S to express anticoagulant activity. (98) This suggests that deficiencies of protein S may also be associated with thrombotic tendencies. Protein S offers an additional intriguing property. Protein S, a regulatory protein of the coagulation system, is found both free and associated with C4BP, a regulatory protein of the complement system. The high affinity, very stable interaction between these components (85) suggests that the interaction is likely to be involved in regulation. (89) The importance of the interaction remains to be demonstrated, but clearly this is a potential direct link between major control proteins of the coagulation and complement system. Clinical studies suggest that protein C and/or thrombomodulin might be effective therapeutically. Certainly, protein C supplementation during the onset of oral anticoagulant therapy would be expected to circumvent the transient rapid decrease in protein C levels that may influence the early effectiveness of oral anticoagulants. (119) In addition to the systems clinical importance, protein C, its activation, and its function offer a variety of intriguing biochemical problems. For instance, how does thrombomodulin alter the specificity of thrombin? What is the protein C binding site on the cell surface, and what role does Factor Va or its degradation products play in the formation and regulation of this site? How does protein S facilitate activated protein C anticoagulant activity and what roles do membrane surfaces play in this system? What role does beta-hydroxyaspartic acid play in protein C activation and function? How does activated protein C influence fibrinolytic activity? The answers to these questions will undoubtedly add to our understanding of the fundamental mechanisms involved in regulating blood coagulation.(ABSTRACT TRUNCATED AT 400 WORDS)

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.Review
Indexed MeSH terms1-Carboxyglutamic AcidAmino Acid SequenceAnimalsAnticoagulantsAntithrombin IIIBlood CoagulationBlood Coagulation FactorsBlood ProteinsBlood VesselsCalciumCarrier ProteinsCattle

Zusammenfassung

The protein C anticoagulant pathway provides many new insights into control mechanisms for regulating coagulation. The observation that protein C deficiency is associated with thrombotic tendencies in the heterozygote (106-109) and early, lethal thrombosis in the homozygote (110, 111) points to the...

Warum dies für die Hirudotherapie relevant ist

Diese Übersichtsarbeit untersucht den Protein-C-Antikoagulans-Signalweg, beschreibt die Thrombin-Thrombomodulin-Aktivierung an der Endotheloberfläche, die Abhängigkeit von aktiviertem Protein C von Protein S sowie die Assoziationen von Protein-C-, Protein-S- oder Thrombomodulin-Mangel mit thromboseförderlichen Zuständen. Sie erwähnt zudem potenzielle therapeutische Überlegungen wie die Protein-C-Supplementierung zu Beginn einer oralen Antikoagulanzientherapie und einen möglichen Zusammenhang zwischen Gerinnung und Komplementregulation über die Protein-S-C4BP-Interaktion. Das Abstract befasst sich mit der endogenen Gerinnungsregulation und ist breit relevant für die Hämostase-/Thrombose-Biologie. Es erwähnt weder Blutegel, Hirudin, aus Blutegeln gewonnene Antikoagulanzien noch Hirudotherapie und liefert somit keine direkte Evidenz für Blutegeltherapie oder das Blutegel-Sekretom.

Zitation

Protein C.

Esmon · Progress in hemostasis and thrombosis, 1984

Verwandter klinischer Kontext

Zur ASH-Bibliothek hinzugefügt: May 28, 2026 · Letzte Aktualisierung der Website: 18. Juni 2026

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